
Aurobindo Pharma


Aurobindo Pharma Assistant Manager Interview Questions and Answers
Q1. How risk can mitigate during product development
Risk during product development can be mitigated by identifying potential risks early, creating contingency plans, involving stakeholders, and conducting thorough testing.
Identify potential risks early in the development process
Create contingency plans for identified risks
Involve stakeholders in decision-making to gain different perspectives
Conduct thorough testing to identify and address any potential issues
Regularly review and update risk management strategies throughout th...read more
Q2. Calculation of thermal heat F0 value
F0 value is a measure of thermal heat required to kill microorganisms in food.
F0 value is calculated using the formula F0 = (t-T)/z
t is the time required to heat the food to a specific temperature
T is the reference temperature at which the microorganisms are killed
z is the heat resistance constant of the microorganisms
F0 value is used to determine the sterilization process for canned foods
Q3. How should equipment be handled?
Equipment should be handled with care and according to manufacturer's instructions.
Always follow manufacturer's guidelines for proper handling and maintenance of equipment
Regularly inspect equipment for any signs of damage or wear
Train employees on proper handling procedures to prevent accidents
Store equipment in a safe and secure location when not in use
Use appropriate personal protective equipment when handling hazardous materials or equipment
Q4. Computer system Validation in Injectables.
Computer system validation is a process of ensuring that computer systems used in pharmaceutical manufacturing are operating as intended.
Validation ensures that the computer system is reliable and produces accurate results.
It involves testing the system to ensure it meets regulatory requirements.
Validation is important in injectables as it ensures the safety and efficacy of the product.
Examples of computer systems that require validation in injectables include those used for ...read more
Q5. describe all process and critical parameters.
Process and critical parameters are key elements that define the steps and variables necessary for successful completion of a task or project.
Process refers to the series of steps or actions taken to achieve a specific goal or outcome
Critical parameters are the key variables or factors that have a significant impact on the success of the process
Examples of critical parameters include temperature, pressure, time, and quality standards
Q6. Interact the event and incident
Events are planned occurrences while incidents are unplanned occurrences.
Events are pre-planned and organized, while incidents are unexpected and unplanned.
Events can be positive or negative, while incidents are usually negative.
Examples of events include weddings, conferences, and concerts, while examples of incidents include accidents, natural disasters, and crimes.
Events can be managed and controlled, while incidents require immediate response and management to minimize da...read more
Q7. Reactor éxperience
I have 3 years of experience working with reactors in a chemical plant setting.
Operated and monitored reactor systems to ensure proper functioning
Performed regular maintenance and troubleshooting on reactors
Implemented safety protocols to prevent accidents and ensure compliance with regulations
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